Suppr超能文献

用于蛋白酶糜蛋白酶递送的混合粘蛋白-文石微球。

Hybrid Mucin-Vaterite Microspheres for Delivery of Proteolytic Enzyme Chymotrypsin.

机构信息

Department of Chemistry, Lomonosov Moscow State University, Leninskiye Gory 1-3, Moscow, 119991, Russian Federation.

Federal Research and Clinical Centre of Physical-Chemical Medicine, Malaya Pirogovskaya 1A, Moscow, 119992, Russian Federation.

出版信息

Macromol Biosci. 2022 Jul;22(7):e2200005. doi: 10.1002/mabi.202200005. Epub 2022 May 9.

Abstract

While the enteral delivery of proteolytic enzymes is widely established for combating many diseases as an alternative to antibiotic treatment, their local delivery only emerges as administration route enabling sustained release in a controlled manner on site. The latest requires the development of drug delivery systems suitable for encapsulation and preservation of enzymatic proteolytic activity. This study proposes hybrid microspheres made of mucin and biodegradable porous crystals of calcium carbonate (CC) as the carriers for chymotrypsin (CTR) delivery. CTR is impregnated into CC and hybrid CC/mucin (CCM) microspheres by means of sorption without any chemical modification. The loading of the CC with mucin enhances CTR retention on hybrid microspheres (adsorption capacity of ≈8.7 mg g  vs 4.7 mg g ), recharging crystal surface due to the presence of mucin and diminishing the average pore diameter of the crystals from 25 to 8 nm. Mucin also retards recrystallization of vaterite into nonporous calcite improving stability of CCM microspheres upon storage. Proteolytic activity of CTR is preserved in both CC and CCM microspheres, being pH dependent. Temperature-induced inactivation of CTR significantly diminishes by CTR encapsulation into CC and CCM microspheres. Altogether, these findings indicate promises of hybrid mucin-vaterite microspheres for mucosal application of proteases.

摘要

虽然将蛋白水解酶经肠道给药作为抗生素治疗的替代方法已广泛用于治疗许多疾病,但只有局部给药才能作为管理途径,以在现场以受控方式持续释放。这就需要开发适合于包封和保护酶蛋白水解活性的药物传递系统。本研究提出了一种混合微球,由粘蛋白和生物可降解的多孔碳酸钙晶体(CC)组成,作为胰凝乳蛋白酶(CTR)的载体。CTR 通过吸附浸渍到 CC 和混合 CC/粘蛋白(CCM)微球中,而无需任何化学修饰。粘蛋白负载 CC 增强了混合微球上 CTR 的保留(≈8.7mg g 对 4.7mg g 的吸附容量),由于粘蛋白的存在,重新充电晶体表面,并将晶体的平均孔径从 25nm 减小至 8nm。粘蛋白还延迟了将水碳酸钙重结晶为无孔方解石,从而提高了 CCM 微球在储存时的稳定性。CC 和 CCM 微球中的 CTR 蛋白水解活性得以保留,且该活性依赖于 pH 值。通过将 CTR 包封到 CC 和 CCM 微球中,可显著减少 CTR 因温度诱导而失活。总的来说,这些发现表明混合粘蛋白-水碳酸钙微球有望用于粘膜蛋白酶的应用。

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